22600-85-7

Basic information

• Product Name: (5,5-diMethyltetrahydrofuran-3-yl)Methanol
• Synonyms: (5,5-diMethyltetrahydrofuran-3-yl)Methanol
• CAS NO: 22600-85-7
• Molecular Formula: C₇H₁₄O₂
• Molecular Weight: 130.19
• Mol File: 22600-85-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 207.2±8.0 °C(Predicted)
• Appearance: /
• Density: 0.951±0.06 g/cm3(Predicted)
• PKA: 14.81±0.10(Predicted)
• CAS DataBase Reference: (5,5-diMethyltetrahydrofuran-3-yl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (5,5-diMethyltetrahydrofuran-3-yl)Methanol(22600-85-7)
• EPA Substance Registry System: (5,5-diMethyltetrahydrofuran-3-yl)Methanol(22600-85-7)

Safety Data

• Hazardous Substances Data: 22600-85-7(Hazardous Substances Data)

Usage

General Description

(5,5-dimethyltetrahydrofuran-3-yl)methanol is a chemical compound that is used as a solvent in various industrial processes. It is a derivative of tetrahydrofuran, a cyclic ether, and is commonly used as a substitute for traditional solvents like diethyl ether and tetrahydrofuran due to its low toxicity and high boiling point. The presence of a hydroxyl group in its structure makes it suitable for use in organic synthesis and as a reagent in various chemical reactions. Additionally, its relatively low cost and compatibility with a wide range of organic compounds make it a popular choice for industrial applications. (5,5-diMethyltetrahydrofuran-3-yl)Methanol is flammable and can cause irritation to the skin and eyes, so it must be handled with care and proper safety measures.

Upstream product

• 53308-41-1 2-(2-methylallyl)propane-1,3-diol 
• 50598-40-8 dimethyl (2-methyl-2-propenyl)-propanedioate 
• 1575-67-3 2-(2-methyl-allyl)-malonic acid diethyl ester 

Downstream Products

• 926-56-7 4-methyl-1,3-pentadiene 
• 592-45-0 1,4-hexadiene 
• 926-54-5 trans-2-methyl-1,3-pentadiene 
• 5602-47-1 dimethyl-2,5 cyclopentadiene 
• 763-30-4 2-methyl-1,4-pentadiene 
• 4045-53-8 1,3-dimethylcyclopentadiene 

Relevant articles and documents

A convenient synthesis of 2-alkyl-2-methyltetrahydrofurans from 4- methylalk-4-en-1-ols catalyzed by iodine

Cyclization of 4-methylalk-4-en-1-ols in the presence of a catalytic amount of iodine in dichloromethane gave exclusively 2-alkyl-2- methyltetrahydrofurans under mild conditions in high yields.

Catalytic Synthesis of Saturated Oxygen Heterocycles by Hydrofunctionalization of Unactivated Olefins: Unprotected and Protected Strategies

A mild, general, and functional group tolerant intramolecular hydroalkoxylation and hydroacyloxylation of unactivated olefins using a Co(salen) complex, an N-fluoropyridinium salt, and a disiloxane reagent is described. This reaction was carried out at ro

Intramolecular additions of alcohols and carboxylic acids to inert olefins catalyzed by silver(I) triflate

(Chemical Equation Presented) Intramolecular additions of hydroxyl or carboxyl groups to inert olefins catalyzed by simple silver(I) triflate are described. Good to excellent yields can be obtained for a range of substrates under relatively mild conditions. This reaction represents one of the simplest methods to construct cyclic ethers or lactones.